PE20090954A1 - Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfa - Google Patents
Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfaInfo
- Publication number
- PE20090954A1 PE20090954A1 PE2008001459A PE2008001459A PE20090954A1 PE 20090954 A1 PE20090954 A1 PE 20090954A1 PE 2008001459 A PE2008001459 A PE 2008001459A PE 2008001459 A PE2008001459 A PE 2008001459A PE 20090954 A1 PE20090954 A1 PE 20090954A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- alkyl
- ppar
- methylphenyl
- fluoro
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P9/14—Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pulmonology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Communicable Diseases (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Psychology (AREA)
- Virology (AREA)
- Gastroenterology & Hepatology (AREA)
Abstract
REFERIDA A UN DERIVADO DE ACIDO FENIL-NICOTINICO DE FORMULA (I), DONDE UNO DE A Y D REPRESENTA N Y EL OTRO REPRESENTA CR7; R7 ES H, METILO O ETILO; R1 ES ALQUILO C3-C10, CICLOALQUILO C3-C7, -NRARB, ENTRE OTROS; RA ES H O ALQUILO C1-C3; RB ES ALQUILO C1-C10, CICLOALQUILO C3-C7, ENTRE OTROS; R2 ES ALQUILO C1-C3 OPCIONALMENTE SUSTITUIDO CON FLUOR O CICLOPROPILO; R3 ES H O F; R4 ES H, Cl, F O METILO; R5 ES H, HALOGENO, NITRO, CIANO, METILO, ENTRE OTROS; R6 ES H, F, Cl O METILO. SON COMPUESTOS PREFERIDOS: ACIDO 6-(3-FLUORO-4-METILFENIL)-2-ISOBUTIL-4-(TRIFLUOROMETIL)NICOTINICO, ACIDO 6-(3-FLUORO-4-METILFENIL)-2-ISOPROPOXI-4-(TRIFLUOROMETIL)NICOTINICO, ACIDO 6-(3-FLUORO-4-METILFENIL)-4-ISOBUTIL-2-METILNICOTINICO, ENTRE OTROS. TAMBIEN ESTA REFERIDA A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON MODULADORES DEL RECEPTOR ACTIVADO POR EL PROLIFERADOR DE PEROXISOMA (PPAR-ALFA) Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES CARDIOVASCULARES, ENFERMEDADES METABOLICAS, ENTRE OTRAS
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102007042754A DE102007042754A1 (de) | 2007-09-07 | 2007-09-07 | Substituierte 6-Phenylnikotinsäuren und ihre Verwendung |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20090954A1 true PE20090954A1 (es) | 2009-07-24 |
Family
ID=40032794
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008001459A PE20090954A1 (es) | 2007-09-07 | 2008-08-28 | Acidos 6-fenilnicotinicos sustituidos como moduladores de ppar-alfa |
Country Status (16)
Country | Link |
---|---|
US (1) | US8143411B2 (es) |
EP (1) | EP2197846A1 (es) |
JP (1) | JP2010538025A (es) |
KR (1) | KR20100066545A (es) |
AU (1) | AU2008298021A1 (es) |
BR (1) | BRPI0816372A2 (es) |
CA (1) | CA2698471A1 (es) |
CL (1) | CL2008002537A1 (es) |
DE (1) | DE102007042754A1 (es) |
MX (1) | MX2010002565A (es) |
NZ (1) | NZ583697A (es) |
PA (1) | PA8794401A1 (es) |
PE (1) | PE20090954A1 (es) |
TW (1) | TW200914002A (es) |
UY (1) | UY31310A1 (es) |
WO (1) | WO2009033561A1 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI2774925T1 (sl) | 2005-11-08 | 2017-04-26 | Vertex Pharmaceuticals Incorporated | Heterociklični modulatorji prenašalcev z ATP-vezavno kaseto |
AU2008251504B2 (en) | 2007-05-09 | 2013-07-18 | Vertex Pharmaceuticals Incorporated | Modulators of CFTR |
EP2231606B1 (en) | 2007-12-07 | 2013-02-13 | Vertex Pharmaceuticals Incorporated | Processes for producing cycloalkylcarboxiamido-pyridine benzoic acids |
NZ702159A (en) | 2007-12-07 | 2016-03-31 | Vertex Pharma | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid |
EP2271622B1 (en) | 2008-02-28 | 2017-10-04 | Vertex Pharmaceuticals Incorporated | Heteroaryl derivatives as CFTR Modulators |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
NZ602838A (en) | 2010-04-07 | 2015-06-26 | Vertex Pharma | Pharmaceutical compositions of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid and administration thereof |
US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
US9113629B2 (en) * | 2013-03-15 | 2015-08-25 | Dow Agrosciences Llc | 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides |
MX2016006118A (es) | 2013-11-12 | 2016-07-21 | Vertex Pharma | Proceso para preparar composiciones farmaceuticas para el tratamiento de enfermedades mediadas por regulador de la conductancia transmembrana de la fibrosis quistica (cftr). |
KR102576006B1 (ko) | 2014-11-18 | 2023-09-06 | 버텍스 파마슈티칼스 인코포레이티드 | 고처리량 시험 고성능 액체 크로마토그래피의 수행 방법 |
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US5217982A (en) | 1990-09-25 | 1993-06-08 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Compounds having antihypertensive properties |
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CN1158290C (zh) * | 1996-01-17 | 2004-07-21 | 诺沃挪第克公司 | 稠合1,2,4-噻二嗪与稠合1,4-噻嗪衍生物、其制备方法及用途 |
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KR20010021936A (ko) | 1997-07-16 | 2001-03-15 | 한센 핀 베네드, 안네 제헤르, 웨이콥 마리안느 | 융합된 1,2,4-티아디아진 유도체, 그의 제조와 사용 |
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DE19943634A1 (de) | 1999-09-13 | 2001-04-12 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
DE19943636A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Dicarbonsäurederivate mit pharmazeutischen Eigenschaften |
DE19943639A1 (de) | 1999-09-13 | 2001-03-15 | Bayer Ag | Dicarbonsäurederivate mit neuartigen pharmazeutischen Eigenschaften |
DE19943635A1 (de) * | 1999-09-13 | 2001-03-15 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
AR031176A1 (es) * | 2000-11-22 | 2003-09-10 | Bayer Ag | Nuevos derivados de pirazolpiridina sustituidos con piridina |
DE10110749A1 (de) * | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte Aminodicarbonsäurederivate |
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JP2005531520A (ja) * | 2002-03-28 | 2005-10-20 | メルク エンド カムパニー インコーポレーテッド | 置換2,3−ジフェニルピリジン類 |
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JP2007513058A (ja) | 2003-09-08 | 2007-05-24 | 武田薬品工業株式会社 | ジペプチジルぺプチダーゼ阻害剤 |
WO2005049606A1 (en) * | 2003-11-05 | 2005-06-02 | F. Hoffmann-La Roche Ag | Heteroaryl derivatives as ppar activators |
WO2005049573A1 (en) | 2003-11-05 | 2005-06-02 | F. Hoffmann-La Roche Ag | Phenyl derivatives as ppar agonists |
CA2579002C (en) | 2004-09-02 | 2012-11-27 | Genentech, Inc. | Pyridyl inhibitors of hedgehog signalling |
DE102005027150A1 (de) | 2005-03-12 | 2006-09-28 | Bayer Healthcare Ag | Pyrimidincarbonsäure-Derivate und ihre Verwendung |
NZ561953A (en) | 2005-04-01 | 2011-11-25 | Insa Rouen | New heterocyclic compounds, their preparation and their use as medicaments, in particular as anti-alzheimer agents |
WO2006124874A2 (en) | 2005-05-12 | 2006-11-23 | Kalypsys, Inc. | Inhibitors of b-raf kinase |
US7932270B2 (en) * | 2006-08-01 | 2011-04-26 | Cytokinetics, Inc. | Certain chemical entities, compositions, and methods |
DE102006043519A1 (de) | 2006-09-12 | 2008-03-27 | Bayer Healthcare Ag | 4-Phenoxynikotinsäure-Derivate und ihre Verwendung |
DE102006043520A1 (de) | 2006-09-12 | 2008-03-27 | Bayer Healthcare Ag | 2-Phenoxynikotinsäure-Derivate und ihre Verwendung |
CN101605792A (zh) * | 2007-02-09 | 2009-12-16 | 阿斯利康(瑞典)有限公司 | 氮杂-异吲哚酮和它们作为亲代谢性谷氨酸受体增效剂-613的用途 |
-
2007
- 2007-09-07 DE DE102007042754A patent/DE102007042754A1/de not_active Withdrawn
-
2008
- 2008-08-26 US US12/676,568 patent/US8143411B2/en active Active
- 2008-08-26 BR BRPI0816372-3A2A patent/BRPI0816372A2/pt not_active IP Right Cessation
- 2008-08-26 EP EP08801700A patent/EP2197846A1/de not_active Withdrawn
- 2008-08-26 WO PCT/EP2008/006969 patent/WO2009033561A1/de active Application Filing
- 2008-08-26 MX MX2010002565A patent/MX2010002565A/es active IP Right Grant
- 2008-08-26 CA CA2698471A patent/CA2698471A1/en not_active Abandoned
- 2008-08-26 NZ NZ583697A patent/NZ583697A/en not_active IP Right Cessation
- 2008-08-26 AU AU2008298021A patent/AU2008298021A1/en not_active Abandoned
- 2008-08-26 JP JP2010523302A patent/JP2010538025A/ja not_active Withdrawn
- 2008-08-26 KR KR1020107007500A patent/KR20100066545A/ko not_active Application Discontinuation
- 2008-08-27 UY UY31310A patent/UY31310A1/es not_active Application Discontinuation
- 2008-08-28 CL CL2008002537A patent/CL2008002537A1/es unknown
- 2008-08-28 PE PE2008001459A patent/PE20090954A1/es not_active Application Discontinuation
- 2008-08-28 PA PA20088794401A patent/PA8794401A1/es unknown
- 2008-09-05 TW TW097133999A patent/TW200914002A/zh unknown
Also Published As
Publication number | Publication date |
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KR20100066545A (ko) | 2010-06-17 |
CA2698471A1 (en) | 2009-03-19 |
PA8794401A1 (es) | 2009-07-23 |
EP2197846A1 (de) | 2010-06-23 |
NZ583697A (en) | 2012-04-27 |
WO2009033561A8 (de) | 2010-06-10 |
US8143411B2 (en) | 2012-03-27 |
DE102007042754A1 (de) | 2009-03-12 |
UY31310A1 (es) | 2009-04-30 |
MX2010002565A (es) | 2010-04-30 |
WO2009033561A1 (de) | 2009-03-19 |
JP2010538025A (ja) | 2010-12-09 |
TW200914002A (en) | 2009-04-01 |
CL2008002537A1 (es) | 2009-03-20 |
US20100234432A1 (en) | 2010-09-16 |
AU2008298021A1 (en) | 2009-03-19 |
BRPI0816372A2 (pt) | 2015-02-24 |
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